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rs13133845

From SNPedia

Orientationplus
Stabilizedplus
Make rs13133845(A;A)
Make rs13133845(A;G)
Make rs13133845(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position94673465
is asnp
is mentioned by
dbSNPrs13133845
ebirs13133845
HLIrs13133845
Exacrs13133845
Varsomers13133845
Maprs13133845
PheGenIrs13133845
hapmaprs13133845
1000 genomesrs13133845
hgdprs13133845
ensemblrs13133845
gopubmedrs13133845
geneviewrs13133845
scholarrs13133845
googlers13133845
pharmgkbrs13133845
gwascentralrs13133845
openSNPrs13133845
23andMers13133845
23andMe allrs13133845
SNP Nexus

SNPshotrs13133845
SNPdbers13133845
MSV3drs13133845
GWAS Ctlgrs13133845
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 24529757]
Trait Amyotrophic lateral sclerosis (sporadic)
Title A genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations.
Risk Allele
P-val 6E-6
Odds Ratio NR NR